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Sexual dimorphism in skin immunity is mediated by an androgen-ILC2-dendritic cell axis.

Liang ChiCan LiuInta GribonikaJulia GschwendDan CorralSeong-Ji HanAi Ing LimClaudia A RiveraVerena M LinkAlexandria C WellsNicolas BouladouxNicholas CollinsDjalma S Lima-JuniorMichel EnamoradoBarbara RehermannSophie LaffontJean-Charles GuéryRoxane TussiwandChristoph SchneiderYasmine Belkaid
Published in: Science (New York, N.Y.) (2024)
Males and females exhibit profound differences in immune responses and disease susceptibility. However, the factors responsible for sex differences in tissue immunity remain poorly understood. Here, we uncover a dominant role for type 2 innate lymphoid cells (ILC2) in shaping sexual immune dimorphism within the skin. Mechanistically, negative regulation of ILC2 by androgens leads to a reduction in dendritic cell (DC) accumulation and activation in males, and reduced tissue immunity. Collectively, this work reveals an androgen-ILC2-DC axis in controlling sexual immune dimorphism. Moreover, this work proposes that tissue immune set points are defined by the dual action of sex hormones and the microbiota, with sex hormones controlling the strength of local immunity and microbiota calibrating its tone.
Keyphrases
  • dendritic cells
  • immune response
  • regulatory t cells
  • nk cells
  • mental health
  • soft tissue
  • wound healing
  • cell cycle arrest
  • oxidative stress